HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52516380A>G , CM000674.2:g.52516380A>G | GRCh38 |
NC_000012.11:g.52910164A>G , CM000674.1:g.52910164A>G | GRCh37 |
NC_000012.10:g.51196431A>G | NCBI36 |
NG_008297.1:g.9080T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252242.9:c.1439+257T>C MANE Select | ENSP00000252242.4:n.1439+257T>C | |
ENST00000252242.8:c.1439+257T>C | ENSP00000252242.4:n.1439+257T>C | |
ENST00000548409.5:c.561+257T>C | ||
ENST00000549511.5:n.646+257T>C | ||
ENST00000552629.5:n.1794T>C | ||
NM_000424.3:c.1439+257T>C | NP_000415.2:n.1439+257T>C | |
NM_000424.4:c.1439+257T>C MANE Select | NP_000415.2:n.1439+257T>C |